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Benziodarone (CAS 68-90-6)

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Alternate Names:
(2-Ethyl-3-benzofuranyl)(4-hydroxy-3,5-diiodophenyl)methanone; Algocor; Cardivix; L 2329; NSC 82133; 2329 Labaz; Amplivix
CAS Number:
68-90-6
Molecular Weight:
518.08
Molecular Formula:
C17H12I2O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Benziodarone is a compound that piques interest in the field of organic chemistry, particularly in the context of iodine-containing molecules and their unique properties. While research on benziodarone itself may not be as extensive as other compounds, its structure prompts investigations into the influence of heavy atoms like iodine on molecular behavior and reactivity. Benziodarone is used in studies exploring the concept of halogen bonding, where researchers assess its potential to engage in non-covalent interactions due to the presence of the iodine moiety. Such interactions are relevant for understanding molecular assembly and recognition processes. Additionally, compounds like benziodarone with heavy halogens are of interest in the design of organic semiconductors, where their ability to facilitate charge transfer is valuable for electronic applications. Moreover, the photophysical properties of benziodarone may be studied to gain insights into the role of heavy atoms in influencing the absorption and emission characteristics of organic molecules.


Benziodarone (CAS 68-90-6) References

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  2. Acute uric acid nephropathy by overdosage of benziodarone in a renal transplant recipient.  |  Franco, A., et al. 2002. Nephron. 92: 746-7. PMID: 12372973
  3. Hyperuricemia causes glomerular hypertrophy in the rat.  |  Nakagawa, T., et al. 2003. Am J Nephrol. 23: 2-7. PMID: 12373074
  4. Long-term efficacy of hyperuricaemia treatment in renal transplant patients.  |  Perez-Ruiz, F., et al. 2003. Nephrol Dial Transplant. 18: 603-6. PMID: 12584286
  5. [Pharmacological interaction between flecainide and benziodarone].  |  Lafuente Gormaz, C., et al. 2003. Rev Esp Cardiol. 56: 631-2. PMID: 12783743
  6. [Value of the controlled hypoxia test for the evaluation of the therapeutic activity of anti-angina substances. Application to benziodarone].  |  VASTESAEGER, M., et al. 1962. Presse Med (1893). 70: 2050-2. PMID: 13996458
  7. IODINE-INDUCED HYPOTHYROIDISM DUE TO BENZIODARONE (CARDIVIX).  |  HARRISON, MT. and CAMERON, AJ. 1965. Br Med J. 1: 840. PMID: 14258850
  8. Uric acid: role in cardiovascular disease and effects of losartan.  |  Alderman, M. and Aiyer, KJ. 2004. Curr Med Res Opin. 20: 369-79. PMID: 15025846
  9. Comparison of the effect of amiodarone and benziodarone on thyroxine metabolism and surface ECG.  |  Moulopoulos, SD., et al. 1989. Endocrinol Exp. 23: 269-78. PMID: 2620658
  10. The dependence of biliary methylmercury secretion on liver GSH and ligandin.  |  Magos, L., et al. 1985. Biochem Pharmacol. 34: 301-5. PMID: 3871612
  11. Uricosuric effect of benziodarone in man and laboratory animals: a comparative study.  |  Lemieux, G., et al. 1973. Am J Physiol. 224: 1431-9. PMID: 4197184
  12. Effects of benziodarone on the biliary excretion of bromosulfophthalein and iodipamide.  |  Van Cantifort, J. and Heusgheim, C. 1973. Biochem Pharmacol. 22: 3120-2. PMID: 4761569
  13. Effects of benziodarone on the metabolism and biliary excretion of sulfobromophthalein and related dyes.  |  Priestly, BG. and Plaa, GL. 1969. Proc Soc Exp Biol Med. 132: 881-5. PMID: 5361006

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Benziodarone, 10 mg

sc-503346
10 mg
$388.00